PARP and CHK inhibitors interact to cause DNA damage and cell death in mammary carcinoma cells

被引：54

作者：

Booth, Laurence ^{[1
]}

Cruickshanks, Nichola ^{[1
]}

Ridder, Thomas ^{[1
]}

Dai, Yun ^{[2
]}

Grant, Steven ^{[2
]}

Dent, Paul ^{[1
]}

机构：

[1] Virginia Commonwealth Univ, Dept Neurosurg, Richmond, VA 23284 USA

[2] Virginia Commonwealth Univ, Dept Med, Richmond, VA 23298 USA

来源：

CANCER BIOLOGY & THERAPY | 2013年 / 14卷 / 05期

基金：

美国国家卫生研究院;

关键词：

PARP1; CHK1; DNA damage; ATM; kinase; apoptosis; comet; POLY(ADP-RIBOSE) POLYMERASE INHIBITORS; DOUBLE-STRAND BREAKS; IN-VITRO; MYELOMA CELLS; REPAIR; CHECKPOINT; CYTOTOXICITY; CANCER; POTENTIATION; APOPTOSIS;

D O I：

10.4161/cbt.24424

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

The present studies examined viability and DNA damage levels in mammary carcinoma cells following PARP1 and CHK1 inhibitor drug combination exposure. PARP1 inhibitors [AZD2281 ; ABT888 ; NU1025 ; AG014699] interacted with CHK1 inhibitors [UCN-01 ; AZD7762 ; LY2603618] to kill mammary carcinoma cells. PARP1 and CHK1 inhibitors interacted to increase both single strand and double strand DNA breaks that correlated with increased gamma H2AX phosphorylation. Treatment of cells with CHK1 inhibitors increased the phosphorylation of CHK1 and ERK1/2. Knock down of ATM suppressed the drug-induced increases in CHK1 and ERK1/2 phosphorylation and enhanced tumor cell killing by PARP1 and CHK1 inhibitors. Expression of dominant negative MEK1 enhanced drug-induced DNA damage whereas expression of activated MEK1 suppressed both the DNA damage response and tumor cell killing. Collectively our data demonstrate that PARP1 and CHK1 inhibitors interact to kill mammary carcinoma cells and that increased DNA damage is a surrogate marker for the response of cells to this drug combination.

引用

页码：458 / 465

页数：8